Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28937879 | 0.925 | 0.080 | 16 | 75479230 | missense variant | A/C | snv | 2.2E-04 | 2.2E-04 | 2 | |
rs58162394 | 0.925 | 0.080 | 17 | 40863154 | missense variant | A/C | snv | 2 | |||
rs58918655 | 0.925 | 0.080 | 17 | 40866768 | missense variant | A/C | snv | 2 | |||
rs121917822 | 1.000 | 0.080 | 16 | 75479525 | missense variant | A/C | snv | 8.0E-06 | 2.8E-05 | 1 | |
rs68043642 | 1.000 | 0.080 | 16 | 75479764 | missense variant | A/C | snv | 1 | |||
rs142954809 | 1.000 | 0.080 | 16 | 75479374 | missense variant | A/C;G | snv | 1.2E-05 | 1 | ||
rs72547545 | 1.000 | 0.080 | 16 | 75479509 | missense variant | A/C;G | snv | 2.8E-05 | 1 | ||
rs763075517 | 0.882 | 0.080 | 16 | 75479311 | missense variant | A/G | snv | 1.6E-05 | 7.0E-06 | 3 | |
rs121917824 | 1.000 | 0.080 | 16 | 75479002 | missense variant | A/G | snv | 5.7E-05 | 1.4E-05 | 1 | |
rs1384294258 | 1.000 | 0.080 | 16 | 75478757 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs775742450 | 1.000 | 0.080 | 16 | 75479627 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs57218384 | 0.925 | 0.080 | 17 | 40866783 | missense variant | C/A;G | snv | 2 | |||
rs72547542 | 1.000 | 0.080 | 16 | 75479332 | missense variant | C/A;G | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs72547546 | 1.000 | 0.080 | 16 | 75479539 | missense variant | C/A;G | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs72547547 | 1.000 | 0.080 | 16 | 75479633 | missense variant | C/A;G | snv | 4.0E-06 | 1 | ||
rs58343600 | 0.925 | 0.080 | 17 | 40866760 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs60410063 | 0.925 | 0.080 | 12 | 52791233 | missense variant | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
rs374493344 | 1.000 | 0.080 | 16 | 75479213 | missense variant | C/A;T | snv | 4.1E-06; 8.3E-06 | 1 | ||
rs58038639 | 0.925 | 0.080 | 17 | 40866778 | missense variant | C/G | snv | 4.0E-06 | 2 | ||
rs758259312 | 1.000 | 0.080 | 16 | 75478844 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs5742909 | 0.614 | 0.680 | 2 | 203867624 | upstream gene variant | C/T | snv | 6.7E-02 | 40 | ||
rs886041459 | 0.925 | 0.080 | 16 | 89935140 | missense variant | C/T | snv | 3 | |||
rs752785520 | 0.925 | 0.080 | 16 | 75479180 | missense variant | C/T | snv | 4.2E-06 | 2 | ||
rs377706989 | 1.000 | 0.080 | 16 | 75479215 | missense variant | C/T | snv | 8.3E-06 | 1.4E-05 | 1 |